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rs273585617

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs273585617(C;T)
Make rs273585617(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position88427760
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585617
ebirs273585617
HLIrs273585617
Exacrs273585617
Varsomers273585617
Maprs273585617
PheGenIrs273585617
hapmaprs273585617
1000 genomesrs273585617
hgdprs273585617
ensemblrs273585617
gopubmedrs273585617
geneviewrs273585617
scholarrs273585617
googlers273585617
pharmgkbrs273585617
gwascentralrs273585617
openSNPrs273585617
23andMers273585617
23andMe allrs273585617
SNP Nexus

SNPshotrs273585617
SNPdbers273585617
MSV3drs273585617
GWAS Ctlgrs273585617
Max Magnitude0
ClinVar
Risk rs273585617(T;T)
Alt rs273585617(T;T)
Reference rs273585617(C;C)
Significance Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88494168C>T
CLNSRC ClinVar
CLNACC RCV000114779.1,